6 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NK GRASP SENSOR, MODEL GA001
FDA 510(k)
FDA Class 2
·Orthopedic
RUSCH MICROLARYNGEAL TUBE
FDA 510(k)
FDA Class 2
·Anesthesiology
AXSOS 3 TI LOCKING PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·January 22, 2013
REPAIR CORE SAG SAW
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS KALAMAZOO·Product code DZJ·December 9, 2010
TENDRIL ST
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014